Clonidine contraindications: Difference between revisions

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{{CMG}}
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{{Clonidine}}
{{CMG}}; {{AE}} {{PB}}


'''''For patient information, click [[Clonidinepatient information)|here]]'''''.


===Contraindications===
===Contraindications===
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An excessive rise in blood pressure following discontinuation of Clonidine therapy can be reversed by administration of oral Clonidine hydrochloride or by intravenous [[phentolamine]]. If therapy is to be discontinued in patients receiving a [[beta-blocker]] and Clonidine concurrently, the beta-blocker should be withdrawn several days before the gradual discontinuation of Clonidine.
An excessive rise in blood pressure following discontinuation of Clonidine therapy can be reversed by administration of oral Clonidine hydrochloride or by intravenous [[phentolamine]]. If therapy is to be discontinued in patients receiving a [[beta-blocker]] and Clonidine concurrently, the beta-blocker should be withdrawn several days before the gradual discontinuation of Clonidine.


Because children commonly have gastrointestinal illnesses that lead to [[vomiting]], they may be particularly susceptible to hypertensive episodes resulting from abrupt inability to take medication.
Because children commonly have gastrointestinal illnesses that lead to [[vomiting]], they may be particularly susceptible to hypertensive episodes resulting from abrupt inability to take medication.<ref name="dailymed.nlm.nih.gov">{{Cite web  | last =  | first =  | title = CATAPRES (CLONIDINE HYDROCHLORIDE) TABLET [BOEHRINGER INGELHEIM PHARMACEUTICALS INC.] | url = http://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=d7f569dc-6bed-42dc-9bec-940a9e6b090d | publisher =  | date =  | accessdate = 5 February 2014 }}</ref>
 
 
 
 
 
 
 
 
{{FDA}}




==References==


{{Reflist|2}}


[[Category:Cardiovascular Drugs]]
[[Category:Drugs]]
[[Category:Drugs]]

Revision as of 19:35, 5 February 2014

Clonidine
CATAPRES® FDA Package Insert
Indications and Usage
Dosage and Administration
Dosage Forms and Strengths
Contraindications
Warnings and Precautions
Adverse Reactions
Drug Interactions
Use in Specific Populations
Overdosage
Description
Clinical Pharmacology
Nonclinical Toxicology
Clinical Studies
How Supplied/Storage and Handling
Patient Counseling Information
Labels and Packages
CLONIDINE patch ® FDA Package Insert
Indications and Usage
Dosage and Administration
Dosage Forms and Strengths
Contraindications
Warnings and Precautions
Adverse Reactions
Drug Interactions
Use in Specific Populations
Overdosage
Description
Clinical Pharmacology
Nonclinical Toxicology
Clinical Studies
How Supplied/Storage and Handling
Patient Counseling Information
Labels and Packages
DURACLON (clonidine hydrochloride) injection® FDA Package Insert
Indications and Usage
Dosage and Administration
Dosage Forms and Strengths
Contraindications
Warnings and Precautions
Adverse Reactions
Drug Interactions
Use in Specific Populations
Overdosage
Description
Clinical Pharmacology
Nonclinical Toxicology
Clinical Studies
How Supplied/Storage and Handling
Patient Counseling Information
Labels and Packages
Clinical Trials on Clonidine
ClinicalTrials.gov

Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]; Associate Editor(s)-in-Chief: Pratik Bahekar, MBBS [2]

For patient information, click here.

Contraindications

Clonidine hydrochloride tablets should not be used in patients with known hypersensitivity to Clonidine.

Warnings for Withdrawal

Patients should be instructed not to discontinue therapy without consulting their physician. Sudden cessation of Clonidine treatment has, in some cases, resulted in symptoms such as nervousness, agitation, headache, and tremor accompanied or followed by a rapid rise in blood pressure and elevated catecholamine concentrations in the plasma.

The likelihood of such reactions to discontinuation of Clonidine therapy appears to be greater after administration of higher doses or continuation of concomitant beta-blocker treatment and special caution is therefore advised in these situations. Rare instances of hypertensive encephalopathy, cerebrovascular accidents and death have been reported after Clonidine withdrawal.

When discontinuing therapy with Clonidine hydrochloride, the physician should reduce the dose gradually over 2 to 4 days to avoid withdrawal symptomatology.

An excessive rise in blood pressure following discontinuation of Clonidine therapy can be reversed by administration of oral Clonidine hydrochloride or by intravenous phentolamine. If therapy is to be discontinued in patients receiving a beta-blocker and Clonidine concurrently, the beta-blocker should be withdrawn several days before the gradual discontinuation of Clonidine.

Because children commonly have gastrointestinal illnesses that lead to vomiting, they may be particularly susceptible to hypertensive episodes resulting from abrupt inability to take medication.[1]


References

  1. "CATAPRES (CLONIDINE HYDROCHLORIDE) TABLET [BOEHRINGER INGELHEIM PHARMACEUTICALS INC.]". Retrieved 5 February 2014.